Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- befree-2016 importedOn "2016-02-19" NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion wasGeneratedBy ECO_0000203 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion wasDerivedFrom befree-2016 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion SIO_000772 12694189 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion evidence source_evidence_literature NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion description "[Lack of fully functional galactokinase is one cause of the inherited disease galactosemia, the main clinical manifestation of which is early onset cataracts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.